Philadelphia, PA, United States of America

Gustavo D Aguirre

USPTO Granted Patents = 15 

 

 

Average Co-Inventor Count = 5.4

ph-index = 4

Forward Citations = 40(Granted Patents)


Location History:

  • Ithaca, NY (US) (1998 - 2012)
  • Philadelphia, PA (US) (2007 - 2019)
  • Media, PA (US) (2021)

Company Filing History:


Years Active: 1998-2025

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15 patents (USPTO):Explore Patents

Title: Gustavo D Aguirre: Innovator in Retinal Treatment

Introduction

Gustavo D Aguirre is a prominent inventor based in Philadelphia, PA, known for his significant contributions to the field of retinal treatment. With a total of 15 patents, Aguirre has focused on developing innovative methods and compositions aimed at treating dominant retinitis pigmentosa, a genetic disorder that leads to progressive vision loss.

Latest Patents

Aguirre's latest patents include groundbreaking work on "Compositions and methods for treatment of dominant retinitis pigmentosa." This patent outlines methods and compositions useful for treating retinitis pigmentosa by delivering interfering RNA to reduce the expression of mutant RHO alleles associated with the condition. Additionally, he has developed AAV vectors for the same purpose, which also involve delivering a replacement RHO coding sequence resistant to the interfering RNA.

Career Highlights

Throughout his career, Aguirre has worked with esteemed organizations such as the Cornell Research Foundation Inc. and the University of Pennsylvania. His work has significantly advanced the understanding and treatment of retinal diseases, making him a key figure in the field of ophthalmology.

Collaborations

Aguirre has collaborated with notable colleagues, including Gregory M Acland and William W Hauswirth, further enhancing the impact of his research and innovations.

Conclusion

Gustavo D Aguirre's contributions to the treatment of retinal disorders exemplify the importance of innovation in medical science. His work continues to inspire advancements in the field and offers hope to those affected by genetic vision loss.

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